FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

TRAUSON BONE SCREW, MODELS HA 3.5 AND 4.5

K Number: K073159 · Decision Jul 23, 2008
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
4
Review Days
258

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
TRAUSON BONE SCREW, MODELS HA 3.5 AND 4.5
K Number
K073159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Trauson (Jiangsu) Medical Instrument Co., Ltd.
Date Received
November 8, 2007
Decision Date
July 23, 2008
Product Code
HWC
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), ordered by most recent decision date.

View all

Other Clearances by Trauson (Jiangsu) Medical Instrument Co., Ltd.

K Number Device Name
K082617 TRAUSON GENERAL SPINAL SYSTEM (GSS)
K081230 TRAUSON INTRAMEDULLARY NAIL
K073432 TRAUSON BONE PLATE